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Multifocal intracranial germinoma with raised tumour markers in serum but not in CSF and with carcinoma in situ of the testis

机译:多灶性颅内生殖瘤,其血清中肿瘤标志物升高,但脑脊液中无肿瘤,睾丸原位癌

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摘要

Primary germ cell tumours (GCTs) are rare malignant neoplasms occurring predominantly in children and adolescents. GCTs appear in the midline of the body, i.e. the gonads, retroperitoneum, mediastinum or the suprasellar and pineal region of the brain. Intracranial germ cell tumours are most often localised in the suprasellar region and may cause pituitary hormone deficits. They arise as a solitary nodule or less commonly as multiple lesions. They are thought to originate from a primordial germ cell that has mismigrated during embryonic development and later undergo malignant transformation. Some GCTs are capable of producing and secreting the tumour markers beta-human chorionic gonadotropin (beta-hCG) and/or alpha-fetoprotein (AFP). Elevated levels of tumour markers in serum and/or spinal fluid indicate the presence of a GCT [1,2].
机译:原发性生殖细胞肿瘤(GCT)是罕见的恶性肿瘤,主要发生于儿童和青少年。 GCT出现在身体的中线,即性腺,腹膜后,纵隔或大脑的上鞍和松果体区域。颅内生殖细胞肿瘤最常位于上鞍区,可能导致垂体激素缺乏。它们以孤立的结节或较少见的多发性病变的形式出现。它们被认为起源于原始生殖细胞,该原始细胞在胚胎发育过程中发生了迁移,随后发生了恶性转化。一些GCT能够产生和分泌肿瘤标记物β-人绒毛膜促性腺激素(β-hCG)和/或甲胎蛋白(AFP)。血清和/或脊髓液中肿瘤标志物的水平升高表明存在GCT [1,2]。

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